Publication | Open Access
Asymmetric Organocatalytic Cascade Michael/Michael/Henry Reaction Sequence: Control of All Stereocenters in One Cyclohexane Skeleton
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Citations
50
References
2012
Year
Novel OrganocatalystsAll StereocentersEngineeringBiochemistryHeterocyclicNatural SciencesQuinine ThioureaOrganic ChemistryCyclohexane SkeletonCatalysisStereoselective SynthesisChemistrySingle Major IsomerAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringCascade Reactions
Abstract The highly diastereo‐ and enantioselective relay cascade Michael/Michael/Henry reaction catalyzed by combination of readily available diphenylprolinol silyl ether and the quinine thiourea in a one‐pot fashion has been developed. Up to 70% yield and up to >99% enantioselectivity of the single major isomer were obtained from the cascade reactions.
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